Evidence map›Paper›PMID 39456119›Full record

ReviewClinical and translational medicine2024

Lactylation in cancer: Mechanisms in tumour biology and therapeutic potentials.

Yipeng He, Tianbao Song, Jinzhuo Ning, Zefeng Wang, Zhen Yin, Pengcheng Jiang, Qin Yuan, Weimin Yu, Fan Cheng

Abstract readReview
In one paragraph

Review in Clinical and translational medicine, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 58 papers.

0numbers the graph read from it
0cells of the map it votes in
58citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

58 citing papers in PubMed.

  1. Research progress of lactylation modification in tumors (Review).Experimental and therapeutic medicine · 2026
    Review
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  6. Lactylation: a novel post-translational modification for cGAS-STING pathway.Inflammation research : official journal of the European Histamine Research Society ... [et al.] · 2026
    Review
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors.

Yipeng HeDepartment of Urology, Renmin Hospital of Wuhan University, Wuhan, Hubei, P.R. China.
Tianbao SongDepartment of Urology, Renmin Hospital of Wuhan University, Wuhan, Hubei, P.R. China.
Jinzhuo NingDepartment of Urology, Renmin Hospital of Wuhan University, Wuhan, Hubei, P.R. China.
Zefeng WangDepartment of Urology, Renmin Hospital of Wuhan University, Wuhan, Hubei, P.R. China.
Zhen YinDepartment of Urology, Renmin Hospital of Wuhan University, Wuhan, Hubei, P.R. China.
Pengcheng JiangDepartment of Urology, Renmin Hospital of Wuhan University, Wuhan, Hubei, P.R. China.
Qin YuanDepartment of Urology, Renmin Hospital of Wuhan University, Wuhan, Hubei, P.R. China.
Weimin YuDepartment of Urology, Renmin Hospital of Wuhan University, Wuhan, Hubei, P.R. China.
Fan ChengDepartment of Urology, Renmin Hospital of Wuhan University, Wuhan, Hubei, P.R. China.ORCID 0000-0002-3471-6221

Funding

National Natural Science Foundation of China #82100806National Natural Science Foundation of China #82170775National Natural Science Foundation of China #82270802National Natural Science Foundation of China #82300766National Natural Science Foundation of China #82370765National Natural Science Foundation of China #82372966
6 · The paper itself

Abstract

Lactylation, a recently identified form of protein post-translational modification (PTM), has emerged as a key player in cancer biology. The Warburg effect, a hallmark of tumour metabolism, underscores the significance of lactylation in cancer progression. By regulating gene transcription and protein function, lactylation facilitates metabolic reprogramming, enabling tumours to adapt to nutrient limitations and sustain rapid growth. Over the past decade, extensive research has revealed the intricate regulatory network underlying lactylation in tumours. Large-scale sequencing and machine learning have confirmed the widespread occurrence of lactylation sites across the tumour proteome. Targeting lactylation enzymes or metabolic pathways has demonstrated promising anti-tumour effects, highlighting the therapeutic potential of this modification. This review comprehensively explores the mechanisms of lactylation in cancer cells and the tumour microenvironment. We expound on the application of advanced omics technologies for target identification and data modelling within the lactylation field. Additionally, we summarise existing anti-lactylation drugs and discuss their clinical implications. By providing a comprehensive overview of recent advancements, this review aims to stimulate innovative research and accelerate the translation of lactylation-based therapies into clinical practice. KEY POINTS: Lactylation significantly influences tumour metabolism and gene regulation, contributing to cancer progression. Advanced sequencing and machine learning reveal widespread lactylation sites in tumours. Targeting lactylation enzymes shows promise in enhancing anti-tumour drug efficacy and overcoming chemotherapy resistance. This review outlines the clinical implications and future research directions of lactylation in oncology.

Indexed as

NeoplasmsProtein Processing, Post-TranslationalHumansTumor Microenvironmentclinical translationlactylationpost translational modificationtumour biologytumour microenvironment

Identifiers

PMID39456119
PMCPMC11511673

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.